HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 4-(3,4-diethoxybenzylidene)-2-methyloxazol-5(4H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | 3,4-Diethoxybenzaldehyde | HCID 74847 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(3,4-diethoxybenzylidene)-2-methyloxazol-5(4H)-one | HCID 54433535 | 45% |
Reaction Steps
To acetic anhydride (193 ml) are added 3,4-diethoxybenzaldehyde (234.4 g), N-acetylglycine (95.4 g) and sodium acetate (49.5 g), and the mixture is heated under reflux for one hour, and the reaction mixture is allowed to stand for cooling. The reaction mixture is further allowed to stand in a refrigerator overnight, and then thereto is added water. The mixture is extracted with chloroform, and the extract is washed, dried and concentrated. The residue is crystallized from ethanol to give 4-(3,4-diethoxybenzylidene)-2-methyloxazol-5(4H)-one (100.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05965730 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-9f5164a76cf441b7a949db897de885d5 |
| Source note | uspto-grants-1999_10 |